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Type | Nanomaterials | Drugs delivered | Disease | Findings | Disadvantages | References |
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Lipid-based nanomaterials | Liposomal annamycin | Annamycin | Acute lymphocytic leukemia, acute myeloid leukemia | Bypass multidrug resistance mechanisms of cellular drug resistance | Diarrhea, typhlitis, and nausea | [148] |
Liposomal doxorubicin | Doxorubicin | Non-Hodgkin’s lymphoma | Prolong systemic circulation, a ligand for cell-specific targeting, and an imaging agent for diagnosis | Induce infusion reactions about activating the complement cascade | [149] |
Liposomal vincristine | Vincristine | Non-Hodgkin’s lymphoma | Reduce neurotoxicity and increase dose intensity delivery | The risk of peripheral neuropathy | [150] |
Liposomal cisplatin | Cisplatin | Progressive osteogenic sarcoma metastatic to the lung | High reactivity, affinity to biomolecules, and low release rate at the tumor site | Possible immune-related reactions or the blood clearance in the case of PEGylated liposomes | [151] |
Docetaxel-loaded solid lipid nanomaterials | Docetaxel | Breast cancer Lung metastasis | High stability for at least 120 days | Short lifespan, poor durability, poor encapsulation | [152] |
Cisplatin-loaded solid lipid nanomaterials | Cisplatin | Breast cancer | Overcome dose-related toxicity, enhance targeting | Require additional microwave-assisted equipment | [153] |
Polymeric nanomaterials | HPMA copolymer—DACH platinate | ProLindac | Ovarian cancer | Increase platinum accumulation in tumors via the enhanced permeability and retention effect | Nausea and vomiting | [154] |
Polymer-lipid hybrid nanomaterials | Doxorubicin | Solid tumors | Prolong drug release, enhance systemic half-life, decrease toxicity, and targeted drug delivery | Potential biotoxicity of nanomaterials | [155] |
Poly(ethylene glycol)-block-poly(L-lactic-co-glycolic acid) | Docetaxel | Prostate cancers | Have good biocompatibility and effective cancer cell inhibition ability | Have potential biotoxicity due to slow drug clearance | [156] |
Folic acid-PAMAM dendrimers | Methotrexate | Epithelial cancer | Increase its antitumor activity and markedly decreased its toxicity | The optimal dose of targeted drug has not been definitively established | [157] |
Poly(glycerol-succinic acid) dendrimers | Camptothecin | Various cancers | Enhance anticancer activity | Limit water solubility and resulting suboptimal pharmacokinetics | [158] |
Superparamagnetic iron oxide nanomaterials | Doxorubicin | Liver cancer | Enhance the biological effects of doxorubicin | Certain hepatorenal toxicity | [159] |
AOT-alginate nanomaterials | Doxorubicin | Breast cancer | Enhancement of therapeutic effect | Some cardiotoxicity | [160] |
Glycol chitosan nanomaterials | Doxorubicin | Solid tumors | Exhibit excellent tumor-homing efficacy, an effective strategy to overcome multidrug resistance | Low solubility | [161] |
Inorganic nanomaterials | Anti-HER2 antibody-targeted gold nanomaterials | Nanoshell-assisted infrared photothermal therapy | Metastatic breast cancer | Retain high antimitotic potency, which could contribute to a higher therapeutic index in high EPR tumors | Potential biotoxicity | [162] |
Silica-based nanomaterials | Organotin metallodrug | Breast cancer | Reduce hepatic and renal toxicity | Some hepatic and renal toxicity | [163] |
Aminosilane-coated iron oxide nanomaterials | Thermotherapy | Brain tumors | Low toxicity, the possibility of radical cure | Complex operation, need further exploration | [164] |
Nanocrystalline 2-methoxyestradiol | Panzem NCD | Various cancers | Delivery of poorly water-soluble drug | Fatigue, nausea, mild transaminitis, and dysgeusia | [165, 166] |
ND-biopolymer nanocomposites | Doxorubicin | Liver cancer | Prolong and continue release of antitumor drugs | Complicated technology | [167] |
Special category | Paclitaxel nanomaterials in porous | Paclitaxel | Solid tumors | Favorable preclinical safety and antitumor activity profiles | Fatigue, alopecia, nausea, vomiting, neuropathy, anorexia, and myalgia | [168] |
Albumin-bound nanomaterials | Doxorubicin, methotrexate | Various cancers | Decrease the glycolysis and metabolic tumor volume | Decrease antibody presence in the general circulation, which might lead to undesirable effects | [169] |
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